Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Tiny Red Bumps


Mother of Jibril

Recommended Posts

Mother of Jibril Enthusiast

I tried looking through old posts for something like this... but I can't seem to find anything that matches just right.

I have some tiny, red, itchy bumps on my hands that showed up in the last few days. They're about 1mm in diameter... not on my palms, and I only have about half a dozen. No bumps on the rest of my body. It's too cold for most bug bites (we just had our first snowfall yesterday). Plus, if were something like scabies, wouldn't they have chosen a warmer part of my body? :huh:

I called to make sure our turkey was gluten and corn free... a "halal" brand (the Muslim version of Kosher)... and the guy said it was fine. Now I wonder. :( I've also been constipated and having some mild abdominal pain the last couple of days. Can you get DH on your hands?

I already had a dermatologist appointment scheduled for Friday... I'm just curious to hear any ideas on what this might be.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



mushroom Proficient

I usually have at least one of these intensely itchy little bumps on the backs of my hands and fingers, often several, although none right now. I have no idea what causes them. But then again I am vey much a skin problem kind of person!!

Mother of Jibril Enthusiast
I am vey much a skin problem kind of person!!

Me too! I went straight from teenage acne to adult acne :( I also have halo nevi (places where my skin is reabsorbing a mole) and rosacea. Thankfully, on the gluten-free diet the long-time rash on my buttocks has gone away! :lol: My rosacea is looking better too.

mushroom Proficient

I finally no longer have the rash on my upper arms that my mother used to tell me was caused by not eating my vegetables :P

luciddream928 Explorer

I get those tiny red bumps too. Exactly how you described. I am convinced they have to do with gluten intolerance because when I am accidentally glutened and all my typical symptoms reappear, the rash is soon to follow. I can't even really call it a rash, the bumps cluster together but not all over my hands, just the joints of my fingers and the top of my right foot.

Incidentally, my mother gets these bumps in the exact same places as me, and we have similar digestive problems. Mine are more severe though. Not sure if it's DH per se, but related to gluten, IMHO.

Mother of Jibril Enthusiast
I finally no longer have the rash on my upper arms that my mother used to tell me was caused by not eating my vegetables :P

:lol::lol::lol:

My parents told me the rash on my buttocks was "sweat pimples."

I get those tiny red bumps too. Exactly how you described. I am convinced they have to do with gluten intolerance because when I am accidentally glutened and all my typical symptoms reappear, the rash is soon to follow. I can't even really call it a rash, the bumps cluster together but not all over my hands, just the joints of my fingers and the top of my right foot.

Incidentally, my mother gets these bumps in the exact same places as me, and we have similar digestive problems. Mine are more severe though. Not sure if it's DH per se, but related to gluten, IMHO.

Right! The bumps are around the joints on my hands... not really enough to call it a "rash." When I see my parents next month I'll have to check their hands ;)

Incidentally, I see we share the DQ7 gene. I'm pretty sure I got that one from my dad.

ksymonds84 Enthusiast

I get those too. The last time was an hour after having Mcdonald's frenchfries (went through drive up and didn't pay attention if they were using a dedicated fryer...my bad). They are usually up and down my fingers with a few on the front of my hands. Mine go away pretty quickly though which is why I think its glutened related but not DH. I also have rosacea, keep waiting for it to go away, glad yours is getting better, it gives me hope!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Mother of Jibril Enthusiast
I also have rosacea, keep waiting for it to go away, glad yours is getting better, it gives me hope!

What really helped with that was taking Betaine HCl with protein meals. I don't know exactly how it reduces inflammation, all I know is that it improves my digestion. Hypochlorhydria (low stomach acid) is one cause of rosacea. For the first time in years I don't look like I have a sunburn on my face! :) I still flush very easily, but it goes away in a few hours.

mushroom Proficient
I also have rosacea, keep waiting for it to go away, glad yours is getting better, it gives me hope!

My rosacea has gone away too. Now it only comes back with a glass of wine.

ksymonds84 Enthusiast
What really helped with that was taking Betaine HCl with protein meals. I don't know exactly how it reduces inflammation, all I know is that it improves my digestion. Hypochlorhydria (low stomach acid) is one cause of rosacea. For the first time in years I don't look like I have a sunburn on my face! :) I still flush very easily, but it goes away in a few hours.

Good info, I will check into it!

ksymonds84 Enthusiast
My rosacea has gone away too. Now it only comes back with a glass of wine.

I'm fine with a little white wine but if I drink red, I look like rudolph! :lol:

zeta-lilly Apprentice
I finally no longer have the rash on my upper arms that my mother used to tell me was caused by not eating my vegetables :P

I've always had little red bumps on my upper arms. So does my dad and a friend of mine (who has pretty severe colitis). They're not itchy or anything. Is that what you're talking about or it is that Dermatitis herpetiformis? I never thought about it being related, but I haven't been gluten free long.

mushroom Proficient
I've always had little red bumps on my upper arms. So does my dad and a friend of mine (who has pretty severe colitis). They're not itchy or anything. Is that what you're talking about or it is that Dermatitis herpetiformis? I never thought about it being related, but I haven't been gluten free long.

Yeah, those were what I had on my upper arms. Different from the itchy ones on my hands, and definitely not DH.

julirama723 Contributor

Aren't those little red bumps (on the arms) Keratosis Pilaris? I have those. They went away for a while (when I was grain-free) but now they're back.

Ugh, also had the butt bumps. Those are THE WORST!

Mother of Jibril--I think you'd posted in a different topic that there might be a relation between KP and celiac? I've read quite a few Celiac/Gluten-Intolerant people also have KP! Do you think the bumps on your hands are KP?

julirama723 Contributor

Oh, threadjack--question about the rosacea--how do you know if it's rosacea and not just rosy cheeks?

My doctor tested me for lupus because my face was so red. I have one sip of wine and I look like Rudolph, too.

Mother of Jibril Enthusiast
Ugh, also had the butt bumps. Those are THE WORST!

Mother of Jibril--I think you'd posted in a different topic that there might be a relation between KP and celiac? I've read quite a few Celiac/Gluten-Intolerant people also have KP! Do you think the bumps on your hands are KP?

I did see that post about keratosis pilaris... very interesting! It sounds exactly like the "arm rash" that other people on this thread have described. I don't think that's what my bumps are though, since I don't have hair follicules around the joints on my hands.

The "butt bumps" ARE annoying! The worst for me was taking a bath... it hurt to sit on the hard surface, and then the bumps would get inflamed from the heat and stick to the tub. :angry: I'm planning to ask the dermatologist about those too.

Oh, threadjack--question about the rosacea--how do you know if it's rosacea and not just rosy cheeks? My doctor tested me for lupus because my face was so red.

Good question! This diagnosis came from my dermatologist. I went to her because I thought I might have vitiligo. In addition to the white spots on my hands (halo nevi), I also pointed out that the skin around my eyes was really pale compared to the rest of my face :ph34r: (Not just rosy cheeks from sunburn or being outside... I looked like that all the time). She checked me with a Wood's lamp and said it's not vitiligo... she suggested rosacea and gave me a Rx for Finacea. I really hate trying new products on my face because my skin is SO sensitive, but it actually helped. Now that I'm corn and gluten-free and taking Betaine HCl with protein meals, I don't even need to use the Finacea!

You're absolutely right that the redness of lupus and rosacea can look similar. I wonder if there's any connection. My ANA was 33, not high enough to be positive for lupus, but definitely showing some autoimmune activity. One of my aunts has lupus... it's associated with the DQ7 gene.

  • 2 weeks later...
Mother of Jibril Enthusiast

OK... so the tiny red bumps on my hands started drying up about a week after I got glutened (on Thanksgiving <_< ).

I got glutened again on Monday (darn holidays!!) and the bumps are back... only this time, I'm also using some new shampoos that my dermatologist prescribed for yeast overgrowth on my scalp. My scalp is fine (I don't think the shampoos have gluten), but the daily showers are killing my skin! The bumps have spread up my arms and are SO itchy. Grrrr.

I'm going to call the dermatologist's office tomorrow and ask what they recommend. There's no way I'm going to last for the next six weeks on this regimen. :angry:

I can hardly wait until the holidays are over so I can go on the SCD. For now I'm just eating as little processed food as possible.

fedora Enthusiast

this was one of my worst symptoms. My little fluid filled blisters were on my palms and fingers. they got so bad that they ate my hand. It was terrible. I got staph and strep in them and could only use my thumb and forefinger. talk about scary. I took antibiotics and used steriods. The rash got better. But when I went off wheat it completely went away. when I would eat wheat, it would come back.

Now I only get them when my digestion gets messed up, but only a few at a time. I don't think it is always gluten related. I know people who get them from corn and I think it could be leaky gut related.

My grandmother(dad's mom) also got them and my mother, but my mom's were from soap.

I also would get itchy buttocks that would get bumpy. In fact, I itched everywhere.

my rash was called Dyshidrotic Eczema. there are photos and info on several websites. my dr says it is allergy related. It is connected to nickel allergy too.

I washed my hands as little as possible, showered with gloves and used gloves to wash dishes. fun days those were.

Mother of Jibril Enthusiast

Ahhhh.... yes. I looked at some websites and DE fits my symptoms better than anything I've seen before. Thank you for that suggestion!!

My first outbreak was not too bad. Just a few blisters on my hands. This time it's also on my palms and my feet <_< I took a couple of CC risks and now it looks like I'm paying the price. I'm trying not to scratch... how scary to get a staph infection!

I'm still going to call the dermatologist tomorrow. There's no way I can keep taking showers every day when it's making the itching worse. Maybe she'll have some other suggestion.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,023
    • Most Online (within 30 mins)
      7,748

    Tubbybooboo
    Newest Member
    Tubbybooboo
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.